Works matching IS 14345161 AND DT 2001 AND VI 46 AND IP 4
Results: 12
A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 167, doi. 10.1007/s100380170083
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Effects of hepatic lipase gene promoter nucleotide variations on serum HDL cholesterol concentration in the general Japanese population.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 172, doi. 10.1007/s100380170084
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Insertion and deletion mutations in the dinucleotide repeat region of the Norrie disease gene in patients with advanced retinopathy of prematurity.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 178, doi. 10.1007/s100380170085
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The c-Jun NH[sub 2] -terminal kinase3 (JNK3) gene: genomic structure, chromosomal assignment, and loss of expression in brain tumors.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 182, doi. 10.1007/s100380170086
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The C825T polymorphism in the G-protein β3 subunit gene and diabetic complications in IDDM patients.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 188, doi. 10.1007/s100380170087
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Fabry disease: twenty novel α-galactosidase A mutations causing the classical phenotype.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 192, doi. 10.1007/s100380170088
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Comparative analysis of HLA restriction and cytokine production in hepatitis B surface antigen-specific T cells from low- and high-antibody responders in vaccinated humans.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 197, doi. 10.1007/s100380170089
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Establishment of an optimized set of 406 microsatellite markers covering the whole genome for the Japanese population.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 207, doi. 10.1007/s100380170090
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Mitochondrial DNA polymorphisms in Yunnan nationalities in China.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 211, doi. 10.1007/s100380170091
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Loci on murine chromosomes 7 and 13 that modify the phenotype of the NOA mouse, an animal model of atopic dermatitis.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 221, doi. 10.1007/s100380170092
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Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 225, doi. 10.1007/s100380170093
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Evaluation of RP2 and RP3 genes in an X-linked RP family manifesting loss of central vision and preserved peripheral function.
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- Journal of Human Genetics, 2001, v. 46, n. 4, p. 241, doi. 10.1007/s100380170094
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- Article